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Clinical and procedural predictors of suboptimal myocardial reperfusion in primary percutaneous coronary intervention

BACKGROUND: Suboptimal myocardial perfusion in primary PCI is associated with increased infarct size, left ventricular (LV) dysfunction and higher mortality rates as compared as those with optimal myocardial perfusion. We identified clinical and procedural predictors of suboptimal myocardial reperfu...

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Autores principales: Mahmoud, Adel H., Taha, Nasser M., Baraka, Khaled, Ashraf, Mohamed, Shehata, Sayed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477166/
https://www.ncbi.nlm.nih.gov/pubmed/31032395
http://dx.doi.org/10.1016/j.ijcha.2019.100357
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author Mahmoud, Adel H.
Taha, Nasser M.
Baraka, Khaled
Ashraf, Mohamed
Shehata, Sayed
author_facet Mahmoud, Adel H.
Taha, Nasser M.
Baraka, Khaled
Ashraf, Mohamed
Shehata, Sayed
author_sort Mahmoud, Adel H.
collection PubMed
description BACKGROUND: Suboptimal myocardial perfusion in primary PCI is associated with increased infarct size, left ventricular (LV) dysfunction and higher mortality rates as compared as those with optimal myocardial perfusion. We identified clinical and procedural predictors of suboptimal myocardial reperfusion as judged by myocardial plush grade (MBG) in primary PCI. METHODS AND RESULTS: 100 patients with acute STEMI who underwent primary PCI were prospectively subjected to clinical, ECG, laboratory and angiographic evaluation. Patients were classified into: Optimal myocardial reperfusion group: (n=73) who had final MBG=3. Suboptimal myocardial reperfusion group: (n=27) who had persistent final MBG ≤ 2. Suboptimal myocardial reperfusion group had statistically significant little history of angina prior to MI 5 (18.5%) vs 44 (60.3%), little current aspirin intake 6(22%) vs 38 (52% ), increased blood sugar on admission (240 ± 101 mg/dl vs 171 ± 72 mg/dl), increased total leucocytic count on admission (12.1 ± 3.6 vs 10.2 ± 3.3) 103/mm3, longer reperfusion time (6.1 ± 2.8 vs 4.3 ± 2.1 h ), higher thrombus burden 12 (44.4 % ) vs 13 (17.8 %), higher predilatation pressure (16 ± 2.3 vs 14 ± 1.8 ATM), repeated balloon inflation during predilatation 24 (92.3 % ) vs 46 (69.7%) as compared optimal myocardial reperfusion group, (P < 0.05 for all). CONCLUSION: Longer reperfusion time, repeated balloon inflations, high predilatation pressure> 15 ATM , high thrombus burden, neither history of angina nor aspirin intake prior to AMI, high total leucocytic count > 10103/mm3 and high blood glucose level > 160mg/dl were predictors for persistent suboptimal myocardial reperfusion in primary PCI.
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spelling pubmed-64771662019-04-26 Clinical and procedural predictors of suboptimal myocardial reperfusion in primary percutaneous coronary intervention Mahmoud, Adel H. Taha, Nasser M. Baraka, Khaled Ashraf, Mohamed Shehata, Sayed Int J Cardiol Heart Vasc Original Paper BACKGROUND: Suboptimal myocardial perfusion in primary PCI is associated with increased infarct size, left ventricular (LV) dysfunction and higher mortality rates as compared as those with optimal myocardial perfusion. We identified clinical and procedural predictors of suboptimal myocardial reperfusion as judged by myocardial plush grade (MBG) in primary PCI. METHODS AND RESULTS: 100 patients with acute STEMI who underwent primary PCI were prospectively subjected to clinical, ECG, laboratory and angiographic evaluation. Patients were classified into: Optimal myocardial reperfusion group: (n=73) who had final MBG=3. Suboptimal myocardial reperfusion group: (n=27) who had persistent final MBG ≤ 2. Suboptimal myocardial reperfusion group had statistically significant little history of angina prior to MI 5 (18.5%) vs 44 (60.3%), little current aspirin intake 6(22%) vs 38 (52% ), increased blood sugar on admission (240 ± 101 mg/dl vs 171 ± 72 mg/dl), increased total leucocytic count on admission (12.1 ± 3.6 vs 10.2 ± 3.3) 103/mm3, longer reperfusion time (6.1 ± 2.8 vs 4.3 ± 2.1 h ), higher thrombus burden 12 (44.4 % ) vs 13 (17.8 %), higher predilatation pressure (16 ± 2.3 vs 14 ± 1.8 ATM), repeated balloon inflation during predilatation 24 (92.3 % ) vs 46 (69.7%) as compared optimal myocardial reperfusion group, (P < 0.05 for all). CONCLUSION: Longer reperfusion time, repeated balloon inflations, high predilatation pressure> 15 ATM , high thrombus burden, neither history of angina nor aspirin intake prior to AMI, high total leucocytic count > 10103/mm3 and high blood glucose level > 160mg/dl were predictors for persistent suboptimal myocardial reperfusion in primary PCI. Elsevier 2019-04-19 /pmc/articles/PMC6477166/ /pubmed/31032395 http://dx.doi.org/10.1016/j.ijcha.2019.100357 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Paper
Mahmoud, Adel H.
Taha, Nasser M.
Baraka, Khaled
Ashraf, Mohamed
Shehata, Sayed
Clinical and procedural predictors of suboptimal myocardial reperfusion in primary percutaneous coronary intervention
title Clinical and procedural predictors of suboptimal myocardial reperfusion in primary percutaneous coronary intervention
title_full Clinical and procedural predictors of suboptimal myocardial reperfusion in primary percutaneous coronary intervention
title_fullStr Clinical and procedural predictors of suboptimal myocardial reperfusion in primary percutaneous coronary intervention
title_full_unstemmed Clinical and procedural predictors of suboptimal myocardial reperfusion in primary percutaneous coronary intervention
title_short Clinical and procedural predictors of suboptimal myocardial reperfusion in primary percutaneous coronary intervention
title_sort clinical and procedural predictors of suboptimal myocardial reperfusion in primary percutaneous coronary intervention
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477166/
https://www.ncbi.nlm.nih.gov/pubmed/31032395
http://dx.doi.org/10.1016/j.ijcha.2019.100357
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